Join our dynamic team where innovation and care converge in a culture that values continuous learning, diversity and transformative career development. Underpinned by THRIVE with Zuellig Pharma, our commitment to transforming the way we grow, care and succeed together as one organization, we are dedicated to helping our people make a meaningful impact in healthcare.
Associate, Regulatory Affairs
Requisition ID:
2370
Posting Start Date:
25 Sept 2026
Location:
Sun Valley, Philippines
| 1. Review the IMS/IQVIA tagging of the materials maintained in the system. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 2. Review and align the material description as per standard format . | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 3. Updates and encodes the Material Maintenance Clean-up monitoring file. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 4. Provides assistance on report consolidation on the activities related to Material Maintenance Clean-up. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 5. Performs validation of the Material maintained in the system. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 6. Performs validation of the Material maintained in the system. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 7. Provide updates and reports to the Regulatory Team. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 8. Performs other tasks assigned by the Regulatory Team. |